MAOA is one of two neighboring gene family members that encode Amine oxidase [flavin-containing] A which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin. Mutation of this gene results in Brunner syndrome. This gene has also been associated with a variety of other psychiatric disorders, including antisocial behavior. Alternatively spliced transcript variants encoding multiple isoforms have been observed. 蛋白别名为：MAOA; Amine oxidase [flavin-containing] A; Monoamine oxidase type A; MAO-A;基因ID为：4128；蛋白质ID:P21397
应用类型
WB，IHC-p，ELISA补充：最优的抗体稀释比例需要基于客户实验进行优化.建议的起始稀释比例如下: WB: 1:500-1:2000, IHC-p: 1:100-1:300, ELISA: 1:20000. Not yet tested in other applications.
